US2779787A - Preparation of aromatic phosphinous chlorides - Google Patents

Description

United States Patent PREPARATION OF AROMATIC PHOSPI-HNOUS CHLORIDES William A. Higgins, Cleveland Heights, George R. Norman, Cleveland, and Willis G. Craig, Willonghhy, Shin, assignors to The Lubrizol Corporation, Wieldiiie, flhio, a corporation of Ohio No Drawing. Application August 13, 1954, Serial No. 449,796

Claims. (Cl. 260-543) This invention. relates to a novel method of synthesis of certain phosphorus-containing organic compounds, and in particular to such a method which involves the removal of chlorine from an organic. compound.

It is a principal. object of this invention to provide a process for the preparation of aromatic phosphinous chlorides. Another object is the-provision. of such a process which is both convenient and economical. Other objects of the invention will be apparent from the ensuing description thereof;

To the accomplishment of the foregoing. and related ends, said invention then comprises thefeatureshereinafter fully described and particularly pointed out in the claims, the following description setting forth in detail certain illustrative embodiments of the invention, these being indicative, however, of but a. few of the various ways in which the principle of the invention may be employed.

It has been discovered that an aromatic phosphinous chloride can be prepared by the abstraction of chlorine from an aromatic phosphoranetrioic trichloride. This conversion is illustrated in the following equation:

ArzPCla-a ArzPCH-ZCI The conversion is effected by heating the particular.

prises heating a mixture of an aromatic phosphoranetrioic trichloride of the structure:

r on whereAr and Ar arethe same or differentaromatic radicalseach bound to phosphorus'through a benzenoid carbon atom, and an element selected from the: class consisting of phosphorus, magnesium, potassium, carbon, and

sodium. The by-products; e. g., phosphorus trichloride, 1

sodium chloride, etc. maybe removed from the product with no ditliculty. In those instances where phosphorus is used the by-product phosphorus trichloiide is removed simply by distilling it from the product mixture. In the case of sodiumclfloride this by-productmay be removed by filtering :theproduct-mixture. In some cases, particularly where the aromatic phosphinouschloride is intended to serve as an intermediate for organic synthetic work, it

' may not be necessary to remove these lay-products. In

.. other instances. a particularly purephosphinous chloride 2,779,787 Patented Jan. 29, 1957 "ice Generally it is preferred to use an amount of phosphorus or sodium (or such other. element as the case. may be) slightly in excess of that indicated by the stoichiometry of the above equations. This allows a more efficient utilization of the aromatic phosphoranetrioic trichloride which is inevitably the more expensive reaction component.

The use of a solvent. is permissible and, in fact, for small-scale reactions, is advisable. Closer control of temperature is possible when, a solventis employed, and also losses of materials due to manipulative diificulties are reduced.

The identity ofthe aromatic radicals in aryl phosphoranetrioic trichlorides which may be used in the. process described herein is established as those aromatic radicals which are nonfunctional- By the-term nonfunctional it is meant to designate those. radicals which neither take part directly in the reaction of the herein-described process nor do they have an active influence on the course of this reaction. Such nonfunctional aromatic radicals include single; multiple; and fused-ring aromatic radicals, especially those of the hydrocarbon type, which radicals may be unsubstituted or contain one or more substituent groups; such as, e. g., alkyl, cycloalkyl, halogen, 'allroxy, alkylmercapto, and the like. They may be illustrated by the following specific examples: phenyl, tolyl, xylyl,

ethylphenyl, isopropylphenyl, tert-butylphenyl, tort-amylphenyl, octylphenyl, diisobutylphenyl, =di-('tert-hutyl) phenyl, di-(tert-amyl) phenyl, waxphenyl, kcr'yiphenyl, xenyl naphthyl, a-methylnaphthyl, kerylnaphthyl, chloro' .phenyl, dichlorophenyl, trichlorophenyl, bromophenyl,

chlorotolyl, anisyl, phenetyl, chloroanisyl, etc.

The aromatic phosphoranetrioic trichloridcs are available as starting materials. for this process from the chlorination either of the corresponding aromatic phosphinodithioic acids or theacid chloridesithereof. This chlorination reaction is the subject of copending application Serial No. 406,328, filed January 26, 1954.

The following specific examples are. given to set forth in greater detail the actual. practice of the invention. It

is to be understood, however,.that these are only illustrative and should not be construed as limiting the scope of the invention.

Example 1 yield 2.47 grams ofa fraction boilingat -l40 C./O.3

min. Analysis of. this fraction established its identity as diphenyl phosphinous chloride:

Percent P "use; 13.7 Percent Cl 16.0

Example 2 A naphtha slurry of diphenyl phosphoranetrioic trichloride prepared by the chlorination of 509 grams (2.0 moles) of diphenyl phosphinodithioic acid was treated with 63 grams (2.0 moles) of red phosphorus and the resulting mixture heated with stirring to 200 C. over a period of six hours. Stirring was continued for an additional hour at this temperature. The residue was filtered and the filtrate was distilled to yield 330 grams of a liquid fraction boiling at 103-106 C./0.2 mm. This fraction upon analysis was shown to be substantially pure diphenyl phosphinous chloride.

Example 3 A naphtha slurry of di(chlorophenyl) phosphoranetrioic trichloride prepared by the chlorination of the corresponding phosphino-dithioic acid was treated with 62.5 grams (2.0 moles) of phosphorus and this mixture then heated with stirring to 200 C. over a period of four hours. This temperature Was maintained for an additional two hours with continued stirring.- The residue was allowed to cool and then was filtered and the solid washed with naphtha. The filtrate and naphtha extract were combined and concentrated by evaporation over diminished pressure to yield 375 grams of material having the following analysis:

Percent P 10.0 Percent Cl 37.2 PercentS 1.6

Fractional distillation of the above product yielded 281 grams of substantially pure di-(chloronhenyl) phosphinous chloride boiling at 147-150" C./0.2 mm. and having the following analysis:

Percent P Percent CI Example 4 To a slurry of 337 grams (1.0. mole) of diphenyl phosphoranetrioic trichloride in 500 cc. of toluene at reflux temperature there was added portionwise with stirring 46 grams (2.0 moles) of sodium. When all the sodium had been added, the mixture was refluxed for an additional hour and then filtered and the filtrate concentrated by heating at 100 C./20 mm. The residue was distilled to yield 145 rams of a liouid boiling'at 133- 146 C./2.0 mm. Thisliouid is diphenyl phosphinous chloride as shown by the following analysis:

Percent P- 13.5 Percent Cl 16.0

Example 5 A slurrv of di henyl phosnhnranetrioic trichloride. prepared bv the chlorination of '100 grams 0.4 mole) of diphenyl nh snhinodithioic acid in 100 ml. of toluene, was treated with gr ms (0.42 mole) of magnesium. The magnesium was added portionwise over a period of 1.5 hours at 100-110 C. and each addition caused foaming and evolution of hvdroizen chloride. When all the magnesium had been added, the resultant mixture was stirred for an additional 1.5 hours at 110 C.' A clear liquid was decanted from the cooled product; This liquid was concentrated by evaporation until there remained '25 grams of a brown, non-viscous liquid residue. This was distilled to yield 14 grams of-a colorless liquid boiling at'86-94" C./0.l mm. The following analyses indicated its identity as the desired diphenyl phosphinous chlorider' Percent phosphorus 13.3

Percent chlorine 17.8

Example 6 Diphenyl phosphoranetrioic trichloride was prepared by the chlorination of 50 grams (0.2 mole) of diphenyl Percent phosphorus 13.5 Percent chlorine 16.5

Example 7 A benzene solution of 88 grams (0.4 mole) of diphenyl phosphinous chloride was treated with the theoretical amount of chlorine to produce the corresponding phosphoranetrioic trichloride. This product was treated with 2.4 grams (0.2 mole) of carbon and then freed of benzene by distillation. The residue was heated at -95 C. for 4 hours, whereupon the temperature was increased gradually through a 4-hour period to 210 C.; this latter temperature being maintained for an additional 2 hours.

The resulting mixture was filtered. This filtrate was distilled, yielding 27 grams of a liquid fraction boiling at 89-115 C./0.1 mm. and having the following analyses:

Percent phosphorus 13.5 Percent chlorine 16.3

Other modes of applying the principle of the invention may be employed, change being made as regards the detail described, provided the features stated in any of the following claims, or the equivalent of such, be employed.

We therefore particularly point out and distinctly claim as our invention:

1. The process of preparing aromatic phosphinous chlorides which comprises heating a mixture of an aromatic phosphoranetrioic trichloride having the structure where Ar and Ar are nonfunctional aromatic radicals each bound to the phosphorus atom through a benzenoid carbon atom, and an element selected from the class consisting of phosphorus, magnesium, potassium, carbon, and sodium.

2. The process of claim 1 characterized further in that Ar and Ar are nonfunctional hydrocarbon aromatic radicals.

3. The process of claim 1 characterized further in that Ar and Ar are nonfunctional halogen-substituted aromatic radicals.

4. The process of claim 1 characterized further in that Ar and Ar are chloro-substituted aromatic radicals.

5. The process of claim 1 characterized further in that Ar and Ar are phenyl radicals. I I 6. The process of preparing aromatic phosphinous chlorides which comprises heating at a temperature between C. and 250 C. a mixture of an aromatic phosphoranetrioic trichloride having the structure where Ar and Ar' are nonfunctional aromatic radicals each bound to the phosphorus atom through a benzenoid carbon atom, and an element selected from the class consisting of phosphorus, magnesium, potassium, carbon, and sodium. 1 I i 7. The process of preparing aromatic phosphinous chlorides which comprises heating a mixture of elemental phosphorus and an aromatic phosphoranetrioic trichloride having the structure 9. The process of claim 7 characterized further in that Ar and Ar are nonfunctional chl-oro-substituted aromatic radicals.

10. The process of claim 7 characterized further in 5 that Ar and Ar are phenyl radicals.

References Cited in the file of this patent Kosolapofi Organo-phosphorus Compounds (Wiley 8:

0 Son,, Inc-1950) pgs. 19, 47 and 58.

Claims (1)

1. THE PROCESS OF PREPARING AROMATIC PHOSPHINOUS CHLORIDES WHICH COMPRISES HEATING A MIXTURE OF AN AROMATIC PHOSPHORANETRIOIC TRICHLORIDE HAVING THE STRUCTURE